Premium Nature Hand Sanitizer Recalled for Subpotent Ethanol Content
AMS Packaging is recalling Premium Nature Instant Hand Sanitizer nationwide because FDA analysis found some bottles contain less ethanol than labeled.
What this means for you
Minor labeling or packaging issue, or a voluntary precautionary recall. Risk of harm is low but real — follow the manufacturer's instructions.
Our severity reasoning: This is an FDA Class II recall for a potency defect with no reported illnesses or injuries. The hazard is theoretical—reduced sanitizer effectiveness—without documented adverse health consequences, fitting the 'low-risk precautionary recall' criterion.
Plain-English summary
AMS Packaging Inc. is recalling Premium Nature Instant Hand Sanitizer (ethyl alcohol 65%), 8 oz/236 mL plastic bottles, distributed nationwide. The recall affects all lots.
FDA analysis revealed that some bottles of this product contain less ethanol than the labeled concentration of 65%, making the sanitizer less effective than intended.
Consumers who have purchased this product should stop using it and dispose of it safely.
The recalled product
- Product
- Premium Nature Instant Hand Sanitizer, (ethyl alcohol 65%), 8 oz/ 236 ML plastic bottles; Premium Nature, South Plainfield, NJ. UPC 819192028668
- Manufacturer
- AMS Packaging Inc
- Category
- Drug — Hand Sanitizer
- Hazard
- subpotent
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (1)
- all lots
Distribution
Distributed nationwide across the United States.
Related recalls
Same category
- CriticalWarfarin Tablets Recalled After Mix-Up Between 2.5 mg and 5 mg Strengths
FDA (Drugs) · 2026-07-21
- HighBeak & Skiff Alcohol Antiseptic Sanitizer recalled for acetaldehyde contamination
FDA (Drugs) · 2026-06-17
- SevereCIMZIA injection recalled due to lack of sterility assurance
FDA (Drugs) · 2026-05-27
- SevereAtomoxetine Capsules Recalled Due to Labeling Mix-Up Error
FDA (Drugs) · 2026-05-27
- LowPrimidone Tablets Recalled Due to Cross-Contamination with Acemetacin
FDA (Drugs) · 2026-05-27